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Development of a high-sensitivity chromatographic separation system for pyridylaminated aldopentoses and aldohexoses
Authors:Shin-ichi Nakakita  Kayo Hasehira  Tomohiro Hosokawa  Masaaki Tokuda  Ken Izumori  Kaoru Takegawa  Jun Hirabayashi
Affiliation:1. Department of Functional Glycomics, Life Science Research Center, Kagawa University, 1750-1 Ikenobe, Miki-cho, Kita-gun, Kagawa 761-0793, Japan;2. Kagawa Industry Support Foundation, Kagawa University, 2393 Ikenobe, Miki-cho, Kagawa 761-0795, Japan;3. Department of Cell Physiology, Faculty of Medicine, Kagawa University, 1750-1 Ikenobe, Miki-cho, Kagawa 761-0793, Japan;4. Rare Sugar Research Center, Kagawa University, 2393 Ikenobe, Miki-cho, Kagawa 761-0795, Japan;5. Department of Bioscience and Biotechnology, Faculty of Agriculture, Kyushu University, Fukuoka 812-8581, Japan
Abstract:A rare sugar is considered to be a monosaccharide rarely found in nature. To investigate their natural distribution and biological roles, a robust analytical system must be used to isolate, identify, and quantify them. Herein, we report the development of such a system that can specifically quantify and chromatographically separate four aldopentoses and eight aldohexoses tagged with 2-aminopyridine. Purified monosaccharides derivatized with a pyridylamino moiety (PA–monosaccharides) are first chromatographed over a high-performance anion-exchange resin. But, because two of the PA–aldohexoses used in this study, PA–talose and PA–idose, co-elute with the common saccharides, PA–glucose and PA–mannose, respectively, a second chromatographic step, reversed-phase high-performance liquid chromatography, is used to completely separate them. Thus, as shown by the results of this study, chromatographic separation of PA–monosaccharides is achievable and provides a quantitative measurement of common and rare isomeric aldopentoses and aldohexoses.
Keywords:Rare sugar   Pyridylamination   Fluorescene labeling
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